Acetazolamide

Product NDC

25021-817

11-digit product format

250210817

Labeler code

25021

Product ID

25021-817_3bb05427-5682-4ee2-94b8-6693a4d874c8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

acetazolamide sodium

Dosage form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Route

INTRAVENOUS

Labeler

Sagent Pharmaceuticals

Application

ANDA200880

Marketing category

ANDA

Marketing start

2012-06-15

Marketing end

2019-09-01

Substance

ACETAZOLAMIDE SODIUM

Active strength

500 mg/5mL

Pharmacologic classes

Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record